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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 088059
Company: EPIC PHARMA LLC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
PREDAMIDE PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM 0.5%;10% SUSPENSION/DROPS;OPHTHALMIC Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
07/29/1983 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
12/20/1990 SUPPL-8 Labeling

Label is not available on this site.

09/30/1988 SUPPL-7 Labeling

Label is not available on this site.

03/01/1988 SUPPL-5 Labeling

Label is not available on this site.

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